drugset / Trial / NCT00175877

A Study of the Safety and Effectiveness of Lyophilized Certolizumab Pegol in the Treatment of Signs and Symptoms of Rheumatoid Arthritis and in Prevention of Joint Damage in Patients With Active Rheumatoid Arthritis

NCT00175877 ↗

Phase 3 Completed 857 enrolled UCB Pharma
NaSingle-groupOpen-labelTreatment

Summary

An open ended study in which patients who completed the double-blind study CDP870-027 \[NCT00152386\] are given Certolizumab Pegol (CZP) and assessed for signs and symptoms of Rheumatoid Arthritis (RA).

Timeline

Start
2005-06
Primary completion
2012-02
Completion
2012-02

Outcome

Met primary endpoint

paper Significantly more patients in the certolizumab pegol 200 mg and 400 mg groups achieved an ACR20 response versus placebo (p< or =0.001); PMID 19015207 ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Certolizumab Pegol Protein / enzyme biologic 200 mg Subcutaneous

Indications